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Evaluation of the efficacy and safety of acupuncture combined with Ba Duan Jin in the treatment of neurogenic cervical spondylosis and research on its mechanism of action

Chinese Orthopedics and Traumatology

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000912
Enrollment
Unknown
Registered
2025-05-07
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neurogenic cervical spondylosis

Interventions

acupuncture group:acupuncture
Acupuncture + eight pieces of brocade group:Acupuncture + eight pieces of brocade
"eight pieces of brocade" group (athletics event):eight pieces of brocade

Sponsors

Dongzhimen Hospital of Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1) Age 18~70 years old male or female; 2) Meet the western medical diagnostic criteria of cervical radiculopathy. 2) Meet the western medical diagnostic criteria for nerve root cervical spondylosis; 3) Meet the diagnostic criteria for Qi stagnation and blood stasis in Chinese medicine; and 1) Age 18~70 years old male or female; 2) Meet the western medical diagnostic criteria of radiculopathy; 3) Meet the diagnostic criteria of qi stagnation and blood stasis of radiculopathy in Chinese medicine. 4) The patient himself/herself or his/her guardian agreed to participate in the study and agreed to participate in the study by signing the informed consent form. 5) Ability to complete the questionnaires and test-related examinations; 6) Normal liver and kidney function; 5) Ability to complete the questionnaires and test-related examinations. 6) Normal liver and kidney function. 7) NRS score =3 or above.

Exclusion criteria

Exclusion criteria: 1) patients with serious heart lung liver kidney and other important organs and blood system function abnormalities; 2) patients with moderate to severe cognitive impairment unable to cooperate with the completion of rehabilitation treatment and examination; patients with severe cognitive impairment unable to cooperate with the completion of rehabilitation treatment and examination 2) Patients with moderate-to-severe cognitive impairment who are unable to cooperate with the completion of rehabilitation treatment and examination; 3) Women who are pregnant or breastfeeding at the same time. (iii) Women who are pregnant or breastfeeding at the same time; (iv) Patients who do not have radicular pain. 4) Patients without radicular pain and patients with pure axial neck pain or spinal cord disease; 5) Patients who are participating in other clinical studies; 6) Patients with skin infections localized at the acupuncture points; 7) Use of medication that interferes with the observation of efficacy within 2 weeks prior to randomization including (fulfilling any of the following). 1) taking aspirin or other non-steroidal anti-inflammatory drugs. 2) Topical application of anti-inflammatory analgesic or blood-stasis activating creams. 3) have done massage physical therapy hot compress treatment. 8) active peptic ulcers / bleeding 9) patients with claustrophobia at the same time

Design outcomes

Primary

MeasureTime frame
NRS score improvement rate;Neck Disability Index;

Secondary

MeasureTime frame
SF-36;Inflammation indicators;C2-7SVA\C2-7Cobb\T1-Slope\ROM;fALFF;

Countries

China

Contacts

Public ContactQi Sun

Dongzhimen Hospital of Beijing University of Chinese Medicine

sunqi2001@sina.com13552777065

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Feb 4, 2026